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IOSR Journal of Applied Chemistry (IOSR-JAC)
IOSR Journal of Applied Chemistry (IOSR-JAC)

Theoretical Studies of the Coordination and Stability of Divalent
Theoretical Studies of the Coordination and Stability of Divalent

... listed in Table 5. The closer this sum is to 360°, the closer the metal is to a planar orientation and the better the overlap of orbitals between the metal and the four O atoms associated with the two Al atoms in the ring. If the ring is too small to accommodate the metal, as is the case for the Z4 ...
The Chemistry of Aluminum as Related to Biology and
The Chemistry of Aluminum as Related to Biology and

... Al(OH)3. This result deserves emphasis. For even though the permitted total Al3 at pH 7.4 may reach 8 pinolJL, most appears as Al(OH)4” and only 3 x 10’12 molJL as Al(H20)634. If the gibbsite solubility product constant were used, both allowed concentrations would be 1/30 as great. Like any other li ...
Gas-phase reactivity of glycosides and methyl glycosides with Cu+
Gas-phase reactivity of glycosides and methyl glycosides with Cu+

... consider the case of silver, copper and lead, each of them exhibits a different behavioural pattern. Silver for example, due to (i) strong germicidal properties, (ii) the development of antibiotic resistance in many diseases and (iii) the increase of new strains of bacteria and viruses, currently ar ...
Dynamic ligand-field theory for square planar transition metal
Dynamic ligand-field theory for square planar transition metal

Excited States of Pt(PF3)4 and Their Role in Focused Electron
Excited States of Pt(PF3)4 and Their Role in Focused Electron

... and vibrational frequencies with experimental data 29–31 and with previous calculations 29,32 are provided in the Supporting Information (SI). The best agreement has been achieved with the LDA functional, geometry and vibrational frequencies agree in all cases to better than 5%. The hybrid B3LYP and ...
Transition Metals
Transition Metals

Structural Chemistry of Titanium Alkoxides Substituted by the
Structural Chemistry of Titanium Alkoxides Substituted by the

Some recent coordination chemistry of lead(ll)
Some recent coordination chemistry of lead(ll)

... alcohols was shown to lead to a series of alkoxides with varying structural features. Sterically undemanding alcohols (isopropanol, 2-methoxyethanol) give linear polymeric compounds [Pb(OR)2]~ where the lead exhibits a distorted trigonal bipyramidal structure, bound to four/~2 alkoxide oxygens. More ...
Revista Portuguesa Química - Sociedade Portuguesa de Química
Revista Portuguesa Química - Sociedade Portuguesa de Química

... (Cisplatin can also be considered a prototypical inorganic drug because it contains not one carbon atom, making it truly an inorganic compound!) To design metal complexes which can be reliably transported to a biological area of interest, both the characteristics of the metal and of the ligand(s) in ...
Diverse Chemical Applications of N
Diverse Chemical Applications of N

Synthesis and characterization of titanium(IV) complexes containing
Synthesis and characterization of titanium(IV) complexes containing

A fluoro-bridged dinuclear nickel(II) compound from
A fluoro-bridged dinuclear nickel(II) compound from

... Fig. 1 UV-vis spectrum of complex (1) (curve 1) and the (L) (curve 2) in CH2Cl2. ...
Series S Sensor Chip NTA - GE Healthcare Life Sciences
Series S Sensor Chip NTA - GE Healthcare Life Sciences

... • Prepare the histidine-tagged ligand in running buffer. Concentrations below 0.2 μM (30 μg/mL for a protein of molecular weight 150 000) are normally sufficient. If the capture level is too high there is a risk that the ligand may dissociate too fast during the analysis cycle. • Inject ligand solut ...
articles
articles

Chapter 3 Ligand Effects
Chapter 3 Ligand Effects

... 3.1.1 Studies of ligand effects on Lewis-acid catalysed reactions in water Research on ligand effects in aqueous solution has mainly focused on two types of organic reactions: decarboxylation and hydrolysis reactions. In section 2.1.1 the Lewis-acid catalysis of the decarboxylation of oxaloacetate w ...
n - KOCW
n - KOCW

A-Frame Complexes of Dirhodium Bridged by Dicarbene and
A-Frame Complexes of Dirhodium Bridged by Dicarbene and

... the rotational freedom in the linking groups between the diphosphine or dicarbene ends of these bidentate ligands, complexes bridged by only one of these groups tend to adopt a skewed arrangement3a,7,11 in which the metals are quite widely spaced in order to minimize steric repulsions between the me ...
BSc/MSci Course Unit Examination - QMplus
BSc/MSci Course Unit Examination - QMplus

Electronegativity and Bond Type: Predicting
Electronegativity and Bond Type: Predicting

... reason, the “natural” axial system for viewing the three bond types for binary compounds. Without exception, compounds classified as metallic occur when the value of the element of higher EN has a value less than about 2.2.5 Whenever the value of the element of higher EN is greater than this, the el ...
d-Block Elements
d-Block Elements

... are high. The densities of the second row are high and third row values are even higher. Elements with the highest densities are osmium 22.57 g cm–3 and irridium 22.61 g cm–3. Across a period from left to right atomic volumes decrease and atomic masses increase. Hence the densities also increase acr ...
Werner`s coordination theory
Werner`s coordination theory

Manganese-Substituted Myoglobin: Characterization and Reactivity
Manganese-Substituted Myoglobin: Characterization and Reactivity

... reported for decades, but investigations into the reactivity of transition metal-substituted myoglobin have received little attention. Transition metal complexes display varying reactivities with different transition metals even when the same types of ligands ligate them [26,27]. Therefore, it is re ...
Exam 3 Review Problems
Exam 3 Review Problems

Small Molecule Activation Using Transfer Hydrogenation Catalysts
Small Molecule Activation Using Transfer Hydrogenation Catalysts

< 1 ... 22 23 24 25 26 27 28 29 30 ... 129 >

Spin crossover



Spin Crossover (SCO), sometimes referred to as spin transition or spin equilibrium behavior, is a phenomenon that occurs in some metal complexes wherein the spin state of the complex changes due to external stimuli such as a variation of temperature, pressure, light irradiation or an influence of a magnetic field.With regard to a ligand field and ligand field theory, the change in spin state is a transition from a low spin (LS) ground state electron configuration to a high spin (HS) ground state electron configuration of the metal’s d atomic orbitals (AOs), or vice versa. The magnitude of the ligand field splitting along with the pairing energy of the complex determines whether it will have a LS or HS electron configuration. A LS state occurs because the ligand field splitting (Δ) is greater than the pairing energy of the complex (which is an unfavorable process).Figure 1 is a simplified illustration of the metal’s d orbital splitting in the presence of an octahedral ligand field. A large splitting between the t2g and eg AOs requires a substantial amount of energy for the electrons to overcome the energy gap (Δ) to comply with Hund’s Rule. Therefore, electrons will fill the lower energy t2g orbitals completely before populating the higher energy eg orbitals. Conversely, a HS state occurs with weaker ligand fields and smaller orbital splitting. In this case the energy required to populate the higher levels is substantially less than the pairing energy and the electrons fill the orbitals according to Hund’s Rule by populating the higher energy orbitals before pairing with electrons in the lower lying orbitals. An example of a metal ion that can exist in either a LS or HS state is Fe3+ in an octahedral ligand field. Depending on the ligands that are coordinated to this complex the Fe3+ can attain a LS or a HS state, as in Figure 1.Spin crossover refers to the transitions between high to low, or low to high, spin states. This phenomenon is commonly observed with some first row transition metal complexes with a d4 through d7 electron configuration in an octahedral ligand geometry. Spin transition curves are a common representation of SCO phenomenon with the most commonly observed types depicted in Figure 2 in which γHS (the high-spin molar fraction) is plotted vs. T. The figure shows a gradual spin transition (left), an abrupt transition with hysteresis (middle) and a two-step transition (right). For a transition to be considered gradual, it typically takes place over a large temperature range, even up to several hundred K, whereas for a transition to be considered abrupt, it should take place within 10 K or less.These curves indicate that a spin transition has occurred in a metal complex as temperature changed. The gradual transition curve is an indication that not all metal centers within the complex are undergoing the transition at the same temperature. The abrupt spin change with hysteresis indicates a strong cooperativity, or “communication”, between neighboring metal complexes. In the latter case, the material is bistable and can exist in the two different spin states with a different range of external stimuli (temperature in this case) for the two phenomena, namely LS → HS and HS → LS. The two-step transition is relatively rare but is observed, for example, with dinuclear SCO complexes for which the spin transition in one metal center renders the transition in the second metal center less favorable.There are several types of spin crossover that can occur in a complex; some of them are light induced excited state spin trapping (LIESST), ligand-driven light induced spin change (LD-LISC), and charge transfer induced spin transition (CTIST).
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